• 제목/요약/키워드: Biological Synthesis

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Arthrobacter simplex의 Steroid ${\Delta}^1$-dehydrogenase의 유도와 유도성 스테로이드의 성질 (The Induction of Steroid ${\Delta}^1$-dehydrogenase from Arthrobacter simplex IAM 1660)

  • 배무;오영주;민태경;이미경
    • 한국미생물·생명공학회지
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    • 제19권3호
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    • pp.242-247
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    • 1991
  • Arthrobacter simplex IAM 1660의 스테로이드 $\Delta^1$-dehydrogenase에 대한 각종 steroid의 유도조건과 효과를 검토하였다. 그 결과 시험한 스테로이드 중 hydrocortisone이 가장 큰 효과를 나타냈고 progesterone, prednisolone, prednisone, androstenstendione의 순으로 유도효과를 보였고, 스테롤에 의해서는 유도효과가 낮았다. 유도 스테로이드의 특성으로는 스테로이드 모핵 C-3위가 수산기인 것보다 캐톤기이며 C-4위에 이중결합이 존재하고 스테로이드 D고리의 측쇄가 짧은 것이 유도 효과가 높았다.

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반도체 공정에서 발생하는 폐실리콘 슬러지의 재활용을 통한 실리카 나노입자의 제조 및 합성법에 따른 형상 및 특성 비교 연구 (A Comparative Study on Morphologies and Characteristics of Silica Nanoparticles Recycled from Silicon Sludge Waste of Semiconductor Process Based on Synthesis Methods)

  • 김지원;사민기;추연룡;제갈석;김하영;김찬교;심형섭;윤창민
    • 유기물자원화
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    • 제31권3호
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    • pp.5-13
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    • 2023
  • 본 연구에서는 반도체 공정에서 발생하는 폐실리콘 슬러지를 활용하여 고부가가치의 실리카 나노입자로 합성하는 방법들에 대한 비교 연구를 수행하였다. 상세히는, 폐실리콘 슬러지 내에 존재하는 금속과 유기 불순물을 산세 처리를 통해 제거한 뒤 졸-겔법과 수열합성법을 통해 실리카 나노입자로 제조하였다. 두 가지 합성법을 통해 제조된 실리카 나노입자에 대한 다양한 형상 및 특성 분석을 진행하였다. 그 결과, 졸-겔법으로 제조된 실리카 나노입자는 순도가 높고 균일한 형상으로 합성되었으며, 수열합성법은 수율과 단순한 제조법의 이점을 확인할 수 있었다. 본 비교 연구는 폐실리콘 슬러지에서 실리카 나노입자를 제조하는 두 가지 합성법에 대한 상세한 실험 결과를 제시하여, 반도체 공정에서 발생하는 부산물을 활용한 고부가가치 소재 제조법 정립에 기여할 것으로 기대된다.

Structural Insights for β-Lactam Antibiotics

  • Dogyeoung, Kim;Sumin, Kim;Yongdae, Kwon;Yeseul, Kim;Hyunjae, Park;Kiwoong, Kwak;Hyeonmin, Lee;Jung Hun, Lee;Kyung-Min, Jang;Donghak, Kim;Sang Hee, Lee;Lin-Woo, Kang
    • Biomolecules & Therapeutics
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    • 제31권2호
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    • pp.141-147
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    • 2023
  • Antibiotic resistance has emerged as a global threat to modern healthcare systems and has nullified many commonly used antibiotics. β-Lactam antibiotics are among the most successful and occupy approximately two-thirds of the prescription antibiotic market. They inhibit the synthesis of the peptidoglycan layer in the bacterial cell wall by mimicking the D-Ala-D-Ala in the pentapeptide crosslinking neighboring glycan chains. To date, various β-lactam antibiotics have been developed to increase the spectrum of activity and evade drug resistance. This review emphasizes the three-dimensional structural characteristics of β-lactam antibiotics regarding the overall scaffold, working mechanism, chemical diversity, and hydrolysis mechanism by β-lactamases. The structural insight into various β-lactams will provide an in-depth understanding of the antibacterial efficacy and susceptibility to drug resistance in multidrug-resistant bacteria and help to develop better β-lactam antibiotics and inhibitors.

Cytosine Arabinoside 유도된 PC12 세포의 사망 경로 (Cytosine Arabinoside-Induced PC12 Cell Death Pathway)

  • 양보기;양병환;채영규
    • 생물정신의학
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    • 제5권2호
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    • pp.219-226
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    • 1998
  • Cytosine arabinoside(AraC) inhibits DNA synthesis and ${\beta}$-DNA polymerase, an enzyme involved in DNA repair. This, a potent antimitotic agent, is clinically used as an anticancer drug with side effect of severe neurotoxicity. Earlier reports suggested that inhibition of neuronal survival by AraC in sympathetic neuron may be due to the inhibition of a 2'-deoxycytidine-dependent process that is independent of DNA synthesis or repair and AraC induced a signal that is triggers a cascade of new mRNA and protein synthesis, leading to apoptotic cell death in cultured cerebellar granule cells. The present study would suggest whether caspase family(ICE/CED-3-like protease) involved in AraC-induced apoptosis pathway of PC12 cells. It was observed that treatment of PC12 cells with AraC led to decrease of viability by MTT assay and morphology changes, which did not suggest that AraC induced apoptosis in PC12 cells. The mRNA of caspase-1/caspase-3 were expressed in PC12 cells constitutively, and AraC did not activate caspase family. These results suggest that caspase-1/caspase-3 may not be required for AraC-induced cell death pathway in PC12 cells.

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Preparation Method for Escherichia coliS30 Extracts Completely Dependent upon tRNA Addition to Catalyze Cell-free Protein Synthesis

  • Ahn, Jin-Ho;Hwang, Mi-Yeon;Oh, In-Seok;Park, Kyung-Moon;Hahn, Geun-Hee;Choi, Cha-Yong;Kim, Dong-Myung
    • Biotechnology and Bioprocess Engineering:BBE
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    • 제11권5호
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    • pp.420-424
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    • 2006
  • A simple method for depleting E. coliS30 extracts of endogenous tRNA has been developed. An $ethanolamine-Sepharose^{(R)}$ column equilibrated with water selectively captured the tRNA molecules in E. coli S30 extracts. As a result, S30 extracts filtered through this column became completely dependent upon the addition of exogenous tRNA to mediate cell-free protein synthesis reactions. We anticipate that the procedures developed and described will be particularly useful for in vitro suppression reaction studies designed to introduce unnatural amino acids into protein molecules.

Expression of Recombinant Human Growth Hormone in a Soluble Form in Escherichia coli by Slowing Down the Protein Synthesis Rate

  • Koo, Tai-Young;Park, Tai-Hyun
    • Journal of Microbiology and Biotechnology
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    • 제17권4호
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    • pp.579-585
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    • 2007
  • Formation of inclusion bodies is usually observed when foreign proteins are overexpressed in E. coli. The formation of inclusion bodies might be prevented by lowering the rate of protein synthesis, and appropriate regulation of the protein expression rate may lead to the soluble expression. In this study, human growth hormone (rhGH) was expressed in a soluble form by slowing down the protein synthesis rate, which was controlled in the transcriptional and translational levels. The transcriptional level was controlled by the regulation of the amount of RNA polymerase specific to the promoter in front of the rhGH gene. For lowering the rate of translation, the T7 transcription terminator-deleted vector was used to synthesize the longer mRNA of the target gene because the longer mRNA is expected to reduce the availability of tree ribosomes. In both methods, the percentage of soluble expression increased when the expression rate slowed down, and more than 93% of rhGH expressed was a soluble form in the T7 transcription terminator-deleted expression system.

The inhibitory effect of egg white lysosome extract (LOE) on melanogenesis through ERK and MITF regulation

  • Park, Jung Eun;Hwang, Hyung Seo
    • Journal of Applied Biological Chemistry
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    • 제65권2호
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    • pp.93-99
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    • 2022
  • Lysosome organelle extract (LOE) was derived from egg whites. The lysosome is an intracellular organelle that contains several hydrolysis enzymes. Previous studies have reported that LOE performs important functions, such as melanin de-colorization and anti-melanin production in B16F10 melanoma cells. However, its principal molecular and cellular mechanisms have not been elucidated till date. In non-cytotoxic conditions, LOE significantly inhibited α-MSH induced melanin synthesis of murine B16F10 cells. The anti-melanogenic activity of LOE was mediated by suppressing the mRNA expression of tyrosinase enzyme, tyrosinase related protein-1/2 (TRP-1/2), and microphthalmia-associated transcription factor (MITF) genes. By performing western blot analysis, we found that LOE significantly attenuated melanogenesis. In this case, LOE helped in increasing extracellular receptor kinase (ERK) phosphorylation in α-MSH induced B16F10 cells. Furthermore, MITF is found to be a key regulatory transcription factor in melanin synthesis; it was down-regulated by LOE through ERK phosphorylation. In this experiment, PD98059 (MEK inhibitor) was used to check whether LOE directly regulated the activity of ERK. Although LOE exerted inhibitory effect on melanin synthesis, we could not observe this effect in PD98059-treated α-MSH induced B16F10. These results strongly indicate that LOE is related to ERK activation and MITF degradation in anti-skin pigmentation. Hence, LOE should be utilized as a whitening agent of skin in the near future.

글루타치온의 효소적 생합성에 관계되는 E.coli ${\gamma}-Glutamylcysteine$ Synthetase의 특성 연구 (Studies on the Properties of E. coli ${\gamma}-Glutamylcysteine$ Synthetase in Relation to the Enzymatic Synthesis of Glutathione)

  • 남용석;곽준혁;이세영
    • Applied Biological Chemistry
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    • 제40권6호
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    • pp.478-483
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    • 1997
  • E. coli K-12 균주에서 ${\gamma}-Glutamylcysteine$ synthetase를 정제하고 효소적 방법에 의한 글루타치온 합성에 관련된 특성을 검사하였다. 정제한 효소의 활성은 L-glutamate의 농도가 60 mM 까지 증가와 더불어 증가하였으나, 60 mM L-cysteine 에서는 50% 그리고 45 mM glycine 에서는 40%의 효소활성이 감소되었다. 효소의 활성은 반응산물 중의 하나인 ADP 뿐만 아니라 환원형 글루타치온에 의해서 감소되었다. 그러므로 환원형 글루타치온 뿐만 아니라 glutathione synthetase의 기질인 glycine은 ${\gamma}-glutamylcysteine$ synthetase 활성을 저해하므로 글루타치온 생산을 위해서는 ${\gamma}-glutamylcysteine$ synthetase 반응과 glutathione synthetase의 두 분리된 반응으로 이루어진 생반응계를 고안하는 것이 바람직하다. 또한 글루타치온 합성반응으로 부터 생성되는 ADP는 ${\gamma}-glutamylcysteine$ synthetase의 활성을 감소시키므로 글루타치온 합성을 위해서 ATP 재생계의 도입이 필요하다.

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